vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 5 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-025
Product ID
71288-025_b7b203d8-dec6-49c3-a147-2cfb5f38cbb3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215196
Listing Expiration
2026-12-31
Marketing Start
2022-07-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288025
Hyphenated Format
71288-025
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
vancomycin hydrochloride (source: ndc)
Generic Name
vancomycin hydrochloride (source: ndc)
Application Number
ANDA215196 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/100mL
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71288-025-75) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b7b203d8-dec6-49c3-a147-2cfb5f38cbb3", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["45642a47-4712-4a12-8cf7-ee6c2ab8e6c6"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71288-025-75) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "71288-025-75", "marketing_start_date": "20220727"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "71288-025_b7b203d8-dec6-49c3-a147-2cfb5f38cbb3", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "71288-025", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "5 g/100mL"}], "application_number": "ANDA215196", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}